Dental Electric
Motor Instruction
Content
Forward ---------------------------------------------------------------------------1
1 Introduction --------------------------------------------------------------------1
2 Basic technical parameters ---------------------------------------------------3
3 Product performance structure and composition -------------------------4
4 Main unit interface ------------------------------------------------------------7
5 Function and operation ----------------------------------------------------- 10
6 Safety precautions ----------------------------------------------------------- 13
7 Cleaning, disinfection and sterilization ----------------------------------- 14
8 Troubleshooting -------------------------------------------------------------- 15
9 Storage and transport -------------------------------------------------------- 15
10 After-sales service ---------------------------------------------------------- 16
11 Environment protection --------------------------------------------------- 16
12 Symbol instruction --------------------------------------------------------- 17
13 EMC-Declaration of comformity ---------------------------------------- 17
1
Forward
Guilin Woodpecker Medical Instrument Co., Ltd is a professional
manufacturer researching, developing, and producing dental products.
Woodpecker owns a sound quality control system and two brands,
Woodpecker and DTE. Its main products include Ultrasonic Scaler,
Curing light, Apex locator, Ultrasurgery, Endo Motor, Electric Motor,
etc.
1 Introduction
Dental electric motor for driving dental handpieces for dental
surgery, Mainly used for dental aesthetics restoration, crown breaking,
open marrow preparation, deburring, polishing and other aspects of
power.
1.1 Precautions before operation
Dangers
:
1. To prevent electric shock, do not use a wet hand to pull the power
cord, and please prevent the water from entering the control circuit.
2
.
Keep away from explosives and ammable materials. Do not use
this dental electric motor for patients who are anesthetized with nitrous
oxide.
Warnings:
1. This dental electric motor may malfunction when used in an
environment where electromagnetic interference occurs. This dental
electric motor cannot be installed near the device that releases the
magnetic wave. When using an ultrasonic vibrating device or an
electrode knife in the vicinity, turn o the switch on the dental electric
motor control panel.
2. MT2 requires special precautions for EMC and needs to be
installed and put into use according to the EMC environment.
3. Device with electromagnetic transmitting will aect the normal
operation of MT2. Please do not run both devices at the same time.
4. Do not use it in operating rooms that contain a mixture of
potentially ammable gases.
5. To avoid possible injury or damage to the dental electric motor,
make sure that the motor handpiece (hereinafter referred to as the motor)
is completely stopped when changing the contra-angle. (And the contra-
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angle tool should be replaced by the pedal controller.)
6. A severe impact, such as a drop from high position, can result in
damage to the dental electric motor.
7. Do not try to disassemble the controlling penal or motor.
8. After use, please immediately clean, lubricate and disinfect the
dental handpiece (hereinafter referred to as the handpiece).
9. Do not lubricate the motor. The lubricant can cause overheating
and damage the motor.
10. Do not use a solution with dissolving ability to clean the control
panel.
11. Do not remove the motor cable from the motor.
12. After each operation, turn o the power supply.
1.2 Intended use
Provide driving force of dental handpieces for dental surgery.
1.3 Model
MT2
1.4 Contraindications
1. The hemophilia patient is forbidden to use this equipment.
2. The patients or doctors with heart pacemaker are forbidden to use
this equipment.
3. Heart disease patients and children should be cautious to use the
equipment.
4. Patients with oral and maxillofacial infections, unhealed oral
mucosal diseases, periapical periodontitis, gum disease, periodontal
disease, oral tumors, etc. should be cautious to use this device.
5. Patients with allergic constitution and history of drug allergy are
prohibited from using this device.
6. Patients with mental disturbance should be cautious to use this
device.
7. Patients with severe systemic or systemic diseases such as heart,
liver, kidney, hematopoietic system, digestive system and endocrine
system should be cautious to use this device.
8. Pregnant women or lactating women, women of childbearing age
who have recently had a birth plan should be cautious to use this device.
1.5 Safety requirements
Guilin Woodpecker Medical Instrument Co., Ltd. will not be
3
liable for any direct or indirect damages and losses under the following
conditions:
•The device is used to the unmentioned usages or the usages outside
the scope of application.
•The operator did not use the device with the method in accordance
with the procedures and requirements stipulated in the Instruction
Manual.
•The wiring system of the room where the device is used does
not meet the requirements of appropriate standard and other proper
requirements.
•Assembling, operating, and repairing the equipment without the
authorization of the Woodpecker.
•The environmental conditions in which the equipment is located
or stored do not meet the requirements mentioned in the section on
technical requirements.
2 Basic technical parameters
2.1 Specication of main unit
Model: MT2
Size:165.5mm×129.7mm×77.6mm
Power supply input: 100-240V~ 50/60Hz 2.5A
Power supply output: DC 30V 3.2A
2.2 Motor specication
Model: E-MT
Rotation speed: 2000-40000 rpm
;
Voltage input: DC 24V
Size: Φ22×76.7mm
Tail cord length: 1.8m
2.3 Use environment
2.3.1 Ambient temperature: +5℃ ~ +40℃
2.3.2 Relative humidity: 30% ~ 75%
2.3.3 Atmospheric pressure: 70kPa ~ 106kPa
2.4 Device safety classication
2.4.1 Type of protection against electric shock: Class II equipment
2.4.2 Degree of protection against electric shock: B type applied
part
4
2.4.3 Degree of protection against harmful ingress of water:
Ordinary equipment (IPX0). Not waterproof.
2.4.4 Classied by operation mode: Intermittent operating device
2.4.5 Degree of safety application in the presence of a ammable
anesthetic mixture with air, oxygen, or nitrous oxide: Equipment cannot
be used in the presence of a flammable anesthetic mixture with air,
oxygen, or nitrous oxide.
3 Product performance structure and composition
3.1 Safety requirements during installation
Danger: Equipment is installed on the premise that the installation
must comply with appropriate standards and associated electric safety
requirements.
Danger: Never install the unit in an explosive atmosphere and do
not operate in areas with ammable gases (anaesthetic mixtures, oxygen,
etc.).
Danger: The installation site should be protected from shocks and
splashes of water or other liquids.
DANGER: Do not install the unit near or above the heat source.
It must be installed in a place where the surrounding air is suciently
circulated. There is enough space around it, especially for the exhaust fan
and the back position.
WARNING: Do not place the parts directly under sunlight or
ultraviolet light.
WARNING: This equipment is movable, but please handles with
care.
WARNING: Make sure the connection parts are dry before
connecting the wires to the unit. If necessary, blow to dry it with an air
gun.
3.2 See the packing list for the machine conguration.
It mainly consists of main unit, motor, power adapter, etc.
5
Figure 1
3.3 Front View of the Main Unit
Figure 2
6
3.4 Rear view of the main unit
Figure 3
3.5 Schematic disgram of motor installation
Figure 4
3.5.1 Connect/Disconnect motor and its tail cord
A
Connect, align and insert the motor and motor tail connections,
twist the nut of the motor tail cord.
B
Remove the motor tail cord from the motor, unscrew and
disconnect the motor wire nut, and gently exit the motor tail connector;
3.5.2 Connect/Disconnect motor and contra-angle
A
Insert the motor connecting shaft into the contra-angle, and then
turn the contra-angle till you heard a “click” sound, to ensure accurate
positioning;
B
When removing the contra-angle, pull the contra-angle out of
the motor in parallel.
3.6 Installation steps
3.6.1 Open the package, check whether the items of the equipment
are complete according to the packing list, and place the main unit on the
7
stable surface.
3.6.2 Connect the four-hole handpiece tube to the control box
through the four-hole handpiece connector and tighten it.
3.6.3 Connect the power adapter to the DC adapter connector and
connect the socket to the DC adapter with the power cord.
3.6.4 As shown in Figure 5, align the positioning boss of the motor
tail cord with the positioning groove of the motor tail cord interface and
insert it, and screw the tail cord nut into the motor tail cord interface until
it can not be screwed by hand.
Figure 5
4 Main unit interface
4.1 Main interface
Figure 6
8
4.2 Setting interface
Figure 7
4.3 Manual mode interface
Figure 8
4.4 Interface of calibration mode
Figure 9
9
Figure 10
Enter the setting interface, click the calibration mode touch button,
enter the air pressure calibration interface, click “Start”, and the interface
will pop up as shown in Figure 10. Fully press the foot pedal to until
it displays 100%, and then release the pedal. Till then the calibration is
successful.
4.5 Restore the factory setting
Figure 11
Enter the setting interface, and click the restore factory settings
touch button to enter the restore factory settings interface for conrmation.
In conforming interface, click OK, the interface shown in Figure 11 will
pop up. Select "OK" to restore the original factory settings parameters or
select "Cancel" to quit restoring factory settings.
4.6 Language selecting interface
Figure 12
10
Enter the setting interface, click the language selection touch button
so that the interface shown in Figure 12 will pop up, and select the
desired language. When you click “OK”, the corresponding language
selected.
5 Function and operation
5.1 Install the product correctly according to the product installation
steps, and the operator should face the screen.
5.2 Turn on the power switch on the main unit, the screen will display
and enter the main control interface (Figure 1).
5.3 The electric motor operation is controlled by the foot pedal of the
dental chair.
5.4 Make sure that the pedal control calibration is performed before
using the unit for the rst time.
5.5 Icon description
Icon Name Function
Mode
Select the preset xed
speed.
(P1/P2/P3)
Speed ratio
Select the speed of contra-
angle
(16:1/1:1/1:5)
Speed adjustment Increase speed
Speed adjustment Decrease speed
Store Store the set parameters
Forward/Reverse rotation
Control the forward and
reverse rotation of motor
Speed
Display the set operating
speed
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Setting Enter the setting interface
Manual mode
Enter manual mode
adjusting interface
Calibration Enter calibration interface
Restore factory setting
Restore the system to
factory setting.
Language selection
Enter language setting
interface
Exit
Exit the submenu setting
mode
Start Start to activate the motor.
Stop Stop the motor
LED
Turn on/o the motor
LED.
Speed adjustment
Adjust the speed formerly
set in the manual mode.
Touch the progress bark
to increase or decrease the
speed.
5.6 Basic function adjustment on main unit controlling interface
12
5.6.1 Select speed ratio through touching key “1”. The color of the
key will change when touching the key.
5.6.2 Control the ON and OFF of LED through key “2”.
5.6.3 5Adjust the speed of the motor by touching key “3”. Increase
or decrease speed with key “+” and “-”.
5.6.4 Switch to the forward rotation or reverse rotation by touching
key “4”.
5.6.5 Select the working speed of corresponding mode by touching
key “5”.
5.6.6 Store the set speed ratio, speed, mode, forward rotation/reverse
rotation, and the ON/OFF of LED by touching key “6”.
5.6.7 Enter setting interface by touching key “7”.
5.7 Basic funtion adjustment in setting interface
5.7.1 In setting interface, touch key “8” Manual Mode key to enter
manual mode interface. Under the manual mode state, the rotation of
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motor can be directly controlled without foot pedal. Touch Speed Ratio
key to select corresponding speed ratio. Touch Speed key to adjust the
speed. Touch Start key, Stop key, Forward/Reverse Rotation key, and
LED key to control the output of motor. Touch the Exit key to exit the
manual mode interface.
5.7.2 In setting interface, touch key “9” Calibration key, touch Start
key, and the interface shown in Figure 8
9would pop up. Fully step on
the foot pedal until it displays 100%, and release the foot pedal to nish
the calibration.
5.7.3 In setting interface, touch key “10” Restore Factory Setting
key, click OK to enter interface shown in Figure 10, and decide whether
to restore the factory setting by clicking “OK” or “Cancel” key.
5.7.4 In setting interface, touch key “11” to enter interface shown in
Figure 7 for language selection.
5.7.5 In the setting interface, touch key “12” to exit submenu setting
mode.
6 Safety precautions
Cautions
:
6.1 For repairs and purchase of spare parts, please contact our
authorized supplier.
6.2 The accuracy of the speed monitoring depends on the high-
precision performance of the handpiece installed on the micro motor. If
the handpiece of other manufacturers is used, the actual speed value may
not be displayed correctly. To ensure the actual matching display speed,
please use the matching handpiece.
6.3 Read this operating manual before use and fully understand the
functions of each part.
6.4 Check the operating status of the dental electric motor before
use to conrm that there is no abnormality.
6.5 Test the dental electric motor before use to ensure accurate
operation.
6.6 If the dental electric motor is permanently malfunctioning
(excessive vibration, noise and heat generation, etc.), please immediately
close it and return it to the authorized dealer.
6.7 Clean the control panel with a damp cloth and turn o the power
before cleaning.
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7 Cleaning, disinfection and sterilization
7.1 Cleaning
Cleaning the motor surface with a water-absorbent cloth to remove
any liquid residue from the motor surface and wipe it back and forth 5
times.
7.2 Disinfection
Use a chlorine-free disinfectant to wipe the motor. It is
recommended to use Cavicide disinfectant or 75% alcohol, but do not
soak the motor in the disinfectant.
7.3 Drying
Drying should be conducted after cleaning and disinfection. It is
recommended to use compressed air to dry.
7.4 Sterilization
Before sterilization, first remove the motor, install a sterile plug
and a sterile aluminum sleeve, place the motor in a high pressure steam
sterilization bag, and seal it. And then sterilize it under the temperature
and pressure of 134 ° C (273 ° F) and 2.0 bar ~ 2.3 bar (0.20MPa
~ 0.23MPa) ) for not less than 4 minutes. Drying is needed after
sterilization, The sterilization of the dental contra-angle handpiece is
detailed in the instruction manual of the contra-angle handpiece.
Warnings:
1. Install disinfection plug and disinfection aluminum sleeve at the
motor interface before sterilization. The installation method is shown
above.
15
2. Before sterilization, the tail cord should be removed.
3. Do not lubricate the inside of the motor.
4. The motor can be sterilized repeatedly for at least 250 cycles of
sterilization.
5. Except the motor and contra-angle, the other parts such as main
unit, power adapter and tail cord are not allowed to be sterilized.
8 Troubleshooting
Fault Cause Solution
Error 01
Step on the foot pedal
before turning on the
device, so that the
voltage is too high.
Release the foot pedal
and reboot.
Error 02
The input voltage is too
high or too low.
Check whether the
power adapter is right.
Error 03 Motor abnormality
Check whether the
motor is well connected
or replace the motor.
If the problem still cannot be solved, please contact our local
distributor or our company.
Note: The user must use the original accessories. Please contact our
local dealer or the company for purchase. It is forbidden to use related
accessories of other brands, so as to avoid damage to the electric motor
or other dangers.
9 Storage and transport
9.1 The device should be handled carefully and lightly. Be sure
that it is far from the vibration, and installed or kept in a cool, dry, and
ventilated place.
9.2 Do not store the machine together with articles that is poisonous,
combustible, caustic, or explosive.
9.3 This machine should be stored in a room where the relative
humidity is10%~93%, atmospheric pressure is 70kPa~106kPa, and the
temperature is -20℃~+55℃.
9.4 Excessive impact and shake should be prevented during
transport. Lay it carefully and lightly.
9.5 Do not put it together with dangerous goods during transport.
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9.6 Avoid being exposed to sun, rain, and snow during transport.
10 After-sales service
Since the date of sales, for the device that cannot work normally for
quality problem, with Warranty Card, our company is responsible for the
repair. Please refer to the Warranty Card for details of warranty.
11 Environment protection
Part
Toxic or harmful substances or elements
(Pb) (Hg) (Cd) (Cr6+) (PBB) (PBDE)
Main unit
Motor
handpiece
Power adapter
Dental contra-
angle
Mechanical
elements,
including bolts,
nuts, washers,
etc.
○: Indicates that the content of the toxic substance in all homogeneous
materials of the part is below the limit requirement stipulated in SJ/T-11363-
2006 Limit Requirements for Toxic and Hazardous Substances in Electronic
Information Products.
×: indicates that the content of the toxic substance in at least one of the
homogeneous materials of the part exceeds the limit requirement specied in
SJ/T-11363-2006.
(This product meets EU RoHS environmental protection requirements; there
is currently no mature technology in the world to replace or reduce the content
of lead in electronic ceramics, optical glass, steel and copper alloy.)
According to the Administrative Measures on the Restriction of the Use of
Hazardous Substances in Electric and Electronic Products and the Regulations
on the Management of the Recycling of Waste Electric and Electronic
Products and related standards, please observe the safety and precautions
of the products, and after use, please recycle or dispose this product after
according to the methods in local laws and regulations
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12 Symbol instruction
Mark
Date of manufacture Manufacturer
Type B applied part ClassⅡequipment
Used indoor only Follow instructions for use
Humidity limitation Temperature limitation
Can be autoclaved Ordinary equipment
Appliance compliance WEEE directive
Atmospheric pressure for storage
13 EMC-Declaration of comformity
The device has been tested and homologated in accordance with EN
60601-1-2 for EMC. This does not guarantee in any way that this device
will not be effected by electromagnetic interference Avoid using the
device in high electromagnetic environment.
Serial
number
Cable name
cable length
m
Cable type
1 Power cord (input) 1.2m Unshielded parallel line
2 Power cord (output) 1.2m Unshielded parallel line
3 Handle tail 1.8m Unshielded parallel line
Technical Description Concerning Electromagnetic Emission
Table 1: Declaration - electromagnetic emissions
Guidance and manufacturer’s declaration - electromagnetic emissions
The model MT2 is intended for use in the electromagnetic environment
specied below. The customer or the user of the model MT2 should assure that
it is used in such an environment.
Emissions test Compliance Electromagnetic environment -
guidance
18
RF emissions
CISPR 11
Group 1 The model MT2 uses RF
energy only for its internal
function. Therefore, its
RF emissions are very low
and are not likely to cause
any interference in nearby
electronic equipment.
RF emissions
CISPR11
Class B The model MT2 is suitable
for used in all establishments,
including domestic
establishments and those
directly connected to the public
low-voltage power supply
network that supplies buildings
used for domestic purposes.
Harmonic emissions
lEC 61000-3-2
Class A
Voltage uctuations /
icker emissions
lEC 61000-3-3
Complies
Technical Description Concerning Electromagnetic Immunity
Table 2: Guidance & Declaration - electromagnetic immunity
Guidance & Declaration — electromagnetic immunity
The model MT2 is intended for use in the electromagnetic environment
specied below. The customer or the user of the model MT2 should assure that
It is used in such an environment.
Immunity test IEC 60601
test level
Compliance level Electromagnetic
environment - guidance
Electrostatic
discharge (ESD)
lEC 61000-4-2
±8kV contact
±2, ±4, ±8,
±15kV air
±8kV contact
±2, ±4, ±8, ±15kV
air
Floors should be wood,
concrete or ceramic tile.
If oors are covered with
synthetic material, the
relative humidity should
be at least 30 %.
Electric fast
transient/burst
IEC 61000-4-4
±2kV for power
supply lines
±1kV for Input/
output lines
±2kV for power
supply lines
Mains power quality
should be that of a
typical commercial or
hospital environment.
Surge
lEC 61000-4-5
±0.5, ±1kV line
to line
±0.5, ±1, ±2kV
line to earth
±0.5, ±1kV line to
line
±0.5, ±1, ±2kV
line to earth
Mains power quality
should be that of a
typical commercial or
hospital environment.
19
Voltage
dips, short
interruptions
and voltage
variations on
power supply
input lines
IEC 61000-4-11
<5 % UT
(>95% dip in
UT.)
for 0.5 cycle
<5 % UT
(>95% dip in
UT.)
for 1 cycle
70% UT
(30% dip in UT)
for 25 cycles
<5% UT
(>95 % dip in
UT)
for 250 cycles
<5 % UT
(>95% dip in UT.)
for 0.5 cycle
<5 % UT
(>95% dip in UT.)
for 1 cycle
70% UT
(30% dip in UT)
for 25 cycles
<5% UT
(>95 % dip in UT)
for 250 cycles
Mains power quality
should be that of a
typical commercial or
hospital environment. If
the user of the models
MT2 requires continued
operation during power
mains interruptions, it is
recommended that the
models MT2 be powered
from an uninterruptible
power supply or a
battery.
Power frequency
(50/60 Hz)
magnetic eld
lEC 61000-4-8
30A/m 30A/m Power frequency
magnetic elds should
be at levels characteristic
of a typical location in
a typical commercial or
hospital environment.
NOTE UT is the a.c. mains voltage prior to application of the test level.
Table 3: Guidance & Declaration - electromagnetic immunity concerning
Conducted RF & Radiated RF
Guidance & Declaration - Electromagnetic immunity
The model MT2 is intended for use in.the electromagnetic environment
specied below. The customer or the user of the models MT2 should assure that
it is used in such an environment.
Immunity test IEC 60601
test level
Compliance
level
Electromagnetic environment -
guidance
20
Conducted RF
lEC 61000-4-6
Conducted RF
lEC 61000-4-6
Radiated RF
lEC 61000-4-3
3 Vrms
150 kHz to 80
MHz
6 Vrms
ISM
frequency
band
3 V/m
80 MHz to 2.7
GHz
3V
6V
3V/m
Portable and mobile RF
communications equipment
should be used no closer to any
part of the models MT2, including
cables, than the recommended
separation distance calculated
from the equation applicable to the
frequency of the transmitter.
Recommended separation distance
d=1.2×P
1/2
d=2×P
1/2
d=1.2×P
1/2
80 MHz to 800 MHz
d=2.3×P
1/2
800 MHz to 2.7 GHz
where P is the maximum output
power rating of the transmitter
In watts (W) according to the
transmitter manufacturer and d
Is the recommended separation
distance in meters (m).
Field strengths from xed RF
transmitters, as determined by
an electromagnetic site survey,a
should be less than the compliance
level in each frequency range.b
Interference may occur In the
vicinity of equipment marked with
the following symbol:
NOTE I At 80 MHz end 800 MHz. the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic
propagation is aected by absorption and reection from structures, objects and
people.
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a Field strengths from xed transmitters, such as base stations for radio (cellular/
cordless) telephones and land mobile radios, amateur radio, AM and FM radio
broadcast and TV broadcast cannot be predicted theoretically with accuracy.
To assess the electromagnetic environment due to xed RF transmitters, an
electromagnetic site survey should be considered. If the measured eld strength
in the location in which the model MT2 is used exceeds the applicable RF
compliance level above, the model MT2 should be observed to verify normal
operation. If abnormal performance is observed, additional measures may be
necessary, such as reorienting or relocating the model MT2.
b Over the frequency range 150 kHz to 80 MHz, eld strengths should be less
than 3V/m.
Table 4: Recommended separation distances between portable and mobile
RF communications equipment and the model MT2
Recommended separation distances between
portable and mobile RF communications equipment and the model
MT2
The model MT2 is intended for use in electromagnetic environment in
which radiated RF disturbances is controlled. The customer or the user of the
model MT2 can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment
(transmitters) and the model MT2 as recommended below, according to the
maximum output power of the communications equipment.
Rated maximum
output power
of transmitter
W
Separation distance according to frequency of transmitter
m
150kHz to 80MHz
d=1.2×P1/2
80MHz to 800MHz
d=1.2×P1/2
800MHz to
2,7GHz
d=2.3×P1/2
0,01 0.12 0.12 0.23
0,1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
22
For transmitters rated at a maximum output power not listed above, the
recommended separation distance d in meters (m) can be estimated using the
equation applicable to the frequency of the transmitter, where P is the maximum
output power rating of the transmitter in watts (W) accordable to the transmitter
manufacturer.
NOTE I At 80 MHz and 800 MHz. the separation distance for the higher
frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic
propagation is aected by absorption and reection from structures, objects and
people.
ZMN-SM-415 V1.5- 20210525